RGD:15139968 Rat Genome Database

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Variant: RGD:15139968 -  Homo sapiens

RGD ID: 15139968
RS ID: rs1578439613
ClinVar ID: CV787242
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL21  IL21-AS1  LOC126807147  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 123,541,849
GRCh38 4 122,620,694
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001207006.3:c.204+7C>T
NM_021803.4:c.204+7C>T
NG_031966.2:g.5373C>T
NC_000004.12:g.122620694G>A
More... 		12/19/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:IL21
Accession:NM_021803
Location:INTRON

Gene Symbol:IL21
Accession:NM_001207006
Location:INTRON

Gene Symbol:IL21-AS1
Accession:NR_104126
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000982735 CLINVAR
dbSNP (RS) rs1578439613 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene IL21 CLINVAR
  IL21-AS1 CLINVAR
  LOC126807147 CLINVAR
OMIM 605384 CLINVAR